FDA Device Establishments · JSON-LD · Markdown
FEI 3007080244 · Remanufacture Medical Device Manufacture Medical Device · Status: Active
| FEI Number | 3007080244 |
|---|---|
| Owner / Operator | KLC Services, Inc./Reep (#10024510) |
| Address | 215 US Highway 42 NE, London, OH, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | BXB |
| Regulation § (21 CFR) | 890.5380 |
| Proprietary names | Flexmate K500; Flexmate S500 |
Source: openFDA. Public-domain (CC0).